人 KCNA1 (NM_000217) cDNA克隆

Accession: NM_000217
基因名称: KCNA1
基因别名: EA1; MK1; AEMK; HBK1; HUK1; MBK1; RBK1; KV1.1
基因描述: Homo sapiens potassium voltage-gated channel, shaker-related subfamily, member 1 (episodic ataxia with myokymia) (KCNA1), mRNA.
种属: Human
CDS区长度: 1488 (查看编码区序列)
翻译后氨基酸长度: 495 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G150971 人 KCNA1 (NM_000217) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a voltage-gated delayed potassium channel that is phylogenetically related to the Drosophila Shaker channel. The encoded protein has six putative transmembrane segments (S1-S6), and the loop between S5 and S6 forms the pore and contains the conserved selectivity filter motif (GYGD). The functional channel is a homotetramer. The N-terminus of the channel is associated with beta subunits that can modify the inactivation properties of the channel as well as affect expression levels. The C-terminus of the channel is complexed to a PDZ domain protein that is responsible for channel targeting. Mutations in this gene have been associated with myokymia with periodic ataxia (AEMK). [provided by RefSeq, Jul 2008]